Cook Spectrum Turbo-Ject G23913Recalls & reported problems

Cook Incorporated · Cook Spectrum Turbo-Ject PICC Set Minocycline/Rifampin Impregnated Power Injectable Polyurethane Peripherally Inserted Central Venous Catheter · Class 2 · Implant

All models of Cook Spectrum Turbo-Ject (12)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 3
Deaths reported: 0
Injuries reported: 3
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00827002239135), received between Feb 5, 2015 and Aug 24, 2021 — classified as 3 injuries.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

Break1
Fluid/Blood Leak1
Fracture1
Insufficient Flow or Under Infusion1
Material Deformation1

Patient problems

No Clinical Signs, Symptoms or Conditions1
No Code Available1
Thrombosis1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

InjuryAug 24, 2021Break; Fracture; Material Deformation; Break; Fracture; Material Deformation
ADDITIONAL INFORMATION WAS PROVIDED ON 31AUG2021 INDICATING THAT THE DEVICE WAS REMOVED AND REPLACED WITH ANOTHER TURBO-JECT® DOUBLE LUMEN MINOCYCLINE/RIFAMPIN POWER-INJECTABLE PICC. THE PATIENT HAS NOT HAD ANY FURTHER ISSUES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12360088 ↗
InjuryOct 23, 2018Fluid/Blood Leak; Fluid/Blood Leak
ADDITIONAL INFORMATION WAS RECEIVED WITH THE RECEIPT OF DEVICE ON(B)(6) 2018 . THE DEVICE WAS PLACED IN THE RIGHT BASILICA VEIN ON (B)(6) 2018 AND REMOVED ON (B)(6) 2018 DUE TO LEAKING OBSERVED AT THE WHITE LUMEN. THE DEVICE WAS UTILIZED FOR BLOOD PRODUCTS, CHEMO AND LABS. PATIENT DEMOGRAPHICS AND DEVICE INFORMATION WERE ALSO PROVIDED.
Patient problems: No Code Available
MAUDE report 7997040 ↗
InjuryFeb 5, 2015Insufficient Flow or Under Infusion
DURING A PICC DEEP VEIN INSERTION PROCEDURE, THROMBOSIS (DVT) OCCURRED AND IT WAS NOTICED THAT THERE WAS A VERY HIGH INCIDENCE OF NEEDING CATHETER FLOW BECAUSE THE PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) HAS CLOTTED OFF. ADDITIONAL INFORMATION REQUESTED 01/19/2014, 01/22/2015, 01/27/2015. NO INFORMATION REGARDING PT OUTCOME WAS PROVIDED.
Patient problems: Thrombosis
MAUDE report 4503926 ↗

Device details

UDI-DI	`00827002239135`
Brand	Cook Spectrum Turbo-Ject
Model	G23913
Catalog no.	UPICDS-5.0-CT-NT-ABRM-1111
Company	Cook Incorporated
Product code	LJS · Catheter,intravascular,therapeutic,long-term greater than 30 days
Class	Class 2
FDA submission	None listed
Implant	Yes
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	Not in Commercial Distribution
Record updated	Feb 3, 2022

Device type (GMDN): Peripherally-inserted central venous catheter

A thin, flexible tube intended to be introduced into a peripheral vein and advanced to a central vein for short- to long-term intravascular access to administer medications (antibiotics), chemotherapeutic agents, nutrients, parenteral solutions, pain management fluids, and sometimes for blood sampling, monitoring of blood pressure and temperature, and for power injection of contrast media; it is not primarily intended for extracorporeal blood therapies such as haemodialysis. Also known as a peripherally inserted central catheter (PICC), it typically includes dedicated accessories to facilitate catheter introduction/function (e.g., Luer hubs, stylet). This is a single-use device.

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All Catheter,intravascular,therapeutic,long-term greater than 30 days devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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